Additive for coatings containing metallic nanoparticles and preparation method therefor

ABSTRACT

The present invention relates to a method of obtaining an additive for coatings that contains nanoparticles of one or more compounds, preferably metallic, selected in relation to the property that is desired to be transferred to the coating, which comprises a first pretreatment phase in which the water content of the active agent is reduced, replacing it with a vehicle compatible with the coating, and a second phase in which it is mixed with a resin compatible with the coating, a dispersant and a solvent, which are also compatible with it. The additive produced by this method contains nanoparticles of one or more compounds, preferably metallic, which become dispersed homogeneously in the coating once incorporated therein.

TECHNICAL FIELD OF THE INVENTION

The present invention relates to additives that are used in paints and coatings, for the purpose of endowing them with desirable properties in relation to the final application, in particular the invention relates to an additive that contains nanoparticles of one or more compounds, preferably metallic, where the solvents, dispersants and surfactants that accompany them are selected depending on the nature of the paint or coating.

BACKGROUND OF THE INVENTION

The use of nanoparticulate compounds for modifying properties different from that of the intrinsic nature of paints, varnishes and coatings in general is known and has increased considerably in recent years.

For example, it is known that nanoparticles of metallic silver are used for conferring antibacterial properties on the materials in which they are incorporated, as is shown in the patents cited hereunder.

The use of some metals or their compounds, as agents that help to improve some of the desired properties in products such as coatings, paints and other polymeric mixtures, is common in everyday practice, for example, the use of silver as antibacterial is well known, and it is known that their effect improves substantially when they are of nanometric size. Although materials exist in which nanometric metallic silver is incorporated, said silver is deposited on inert substrates with a size of several microns, resulting in localized zones with a high concentration of nanoparticles.

Zinc oxide is known for its fungicidal effect, and is widely used in personal hygiene articles and skin medications. It is also known that in nanometric sizes it can absorb ultraviolet light, offering protection for materials that contain it. As with all nanometric compounds, better dispersion and controlled particle size offer advantages, since unprotected zones are practically eliminated.

The flame retardant effect of magnesium hydroxide is also known, and it has been observed that in nanometric sizes it offers advantages, for example of transparency, without affecting the mechanical properties of the coating in which it is used. This is embodied in patent application PCT/MX 2007/000046 (Martinez et al., 2007), which relates to a method for the preparation of a flame retardant additive for coatings and the resultant products.

Similarly, the properties of nanoparticles of Ag, Au, Cu, Bi, Mg, Zn, Sb, their oxides, hydroxides, sulfides, chlorides, sulfates, and mixtures thereof, are transferred to the coating of the final application.

Several examples have been found of coatings in which nanoparticles are incorporated to endow them with certain qualities or properties. The main problem to be tackled is the efficient dispersion of the nanoparticles in the application volume, because of the appearance of agglomerates that reduce their effectiveness.

The present invention describes an additive that ensures the homogeneous distribution and efficient dispersion of the nanoparticles throughout the coating. For greater clarity, in this document “additive” means a mixture or combination of components that is added to another substance to give it qualities that it lacks or to improve those that it already possesses. In particular the additive according to the invention is for application in coatings such as paints, varnishes and polymeric mixtures that are fluid at room temperature.

In the prior art there is a great variety of alternatives for incorporating nanoparticles in coatings, and thus provide them with certain properties intrinsic to said nanoparticles, some examples of which are mentioned below.

Patent CN 1850924 (Li, 2006) describes the production of an antibacterial coating containing silver nanoparticles. The additive is prepared using hydroxylated acrylic resin or an emulsion of acrylic acid polymer, starting from a 6% solution of silver nanoparticles in a polyethylene wax. The product obtained in this method cannot be made compatible with other systems and is limited to a maximum concentration of 6%.

Patent CN 1837035 (Wang et al., 2006) gives an account of a method of preparation of a hybrid carbon membrane that contains inorganic nanoparticles. The product of this invention is limited to just one type of application.

Patent JP 2005248136 (Ando, 2005) discusses an additive that contains nanometric silver for coatings, which prevents marine organisms adhering to surfaces. This invention is limited to the removal of marine organisms on surfaces submerged in water and to a paint for marine application.

Patent TW 220398 (Liang, 2004) discusses an additive that contains metallic nanoparticles, but which are synthesized directly in an organic solvent. Application of the product of this invention is limited to materials compatible with organic solvents and that can be synthesized therein.

Patent WO 2003103392 (Norminger et al. 2003) describes a coating that contains antibacterial metallic nanoparticles, but has the limitation that said nanoparticles are on other particles of titanium dioxide.

Publication US20070173564A1 (Sohn et al., 2007) relates to a composition for producing a transparent coating with a photocurable resin, which contains silver nanoparticles. The product of this invention is limited to silver nanoparticles in a photocurable transparent coating.

Publication US2006155033A1 (Sisson, 2006) describes an emulsion used for improving the electrical conductivity between contact surfaces, for example electrical connectors, and for protecting them against the effects of time. This coating is limited to the transfer of electrical properties and to the use of silver nanoparticles.

U.S. Pat. No. 6,855,749B1 (Yadav et al. 2005) is limited to a nanocomposite polymer that is mainly used as a material for biological uses in applications such as vehicles of medicinal products, biomedical devices, and implants of bones or teeth.

U.S. Pat. No. 6,228,904B1 (Yadav et al. 2001) relates specifically to a polymeric composite with nanomaterials with properties of resistivity, the method and the application of the mixture for producing a plastic with electrical properties. The teaching of this document is not directly applicable to fluid mixtures for coatings, as in our case, except that the properties in question are related to the electrical properties.

The additive of the present invention is designed for transferring, to a final coating, biocidal, UV protection, and flame retardant properties, and in general, selected properties intrinsic to the metals and compounds of Ag, Au, Cu, Mg, Zn, Bi, Sb; the additive includes the use of solvents, surfactants, dispersants and resins that make it compatible with the final coating. Said coating with additive ensures perfect distribution and dispersion of the nanoparticles throughout it, without the need for an inorganic substrate. The process for the manufacture of the additive starts from existing nanoparticles of the aforementioned metals and compounds, which can be in aqueous organic media or alternatively as dry powders, and are submitted to a treatment that allows them to be incorporated in coatings used in a wide variety of environmental conditions. The process can be used for obtaining a variety of functionalized additives.

OBJECTS OF THE INVENTION

One object of the present invention is to provide a composition for use as an additive in polymeric mixtures, such as paints, varnishes or coatings of a fluid nature, in which the properties desired in the final application are provided by metallic nanometric particles and their composites, selected specifically.

Another object of the present invention is that the nanoparticles of the additive that confer the properties on the coating are distributed homogeneously in the volume of the coating.

Another object of the present invention is to provide an additive in which the nanoparticles of the additive do not agglomerate, remaining dispersed throughout the shelf life, both of the additive and of the coating in which they are incorporated.

One more object of the present invention is that the properties desired in the coating can be obtained by the appropriate selection of nanoparticles of one or more metals and their compounds.

Yet another object of the present invention is to provide an additive in which the nanoparticles of metal or metal compounds do not require an additional carrier, such as ceramic materials, in order to remain unagglomerated.

These and other objects will become clear, to a person skilled in the art, on reading the description that follows.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a block diagram that represents the process for production of the additive according to the invention.

DETAILED DESCRIPTION OF THE INVENTION

The additive prepared according to the method of the present invention is produced starting from metallic nanoparticles and their composites, with an average particle size that is selected in the range from 1 to 100 nanometers, preferably monodispersed, i.e. having a very narrow size variation, the particle size being a function of the desired application; for example, it is considered that in applications of the medical type, sizes less than 10 nm are preferred, and in UV protection sizes around 60 nm are preferred; and with a purity of at least 95%.

Selection of the material of the nanoparticles to be used in the formulation of the additive of the present invention is closely linked to the property that is desired in the final application, as can be seen from Table 1, which shows some examples that serve for determining the parameters recommended for obtaining the desired effects in the final application.

TABLE 1 Recommended selection of nanoparticles for preparation of the additive. Property Ag° Au° Cu° Bi° Mg(OH)₂ ZnO AgS Bi₂O₃ Sb₂O₅ A X X X X B X X X C X X D X X X E X X X X X X F X X X X Where: A: biocidal properties, such as bactericide, fungicide and algicide. B: UV protection. C: Flame retardant. D: Fungicide. E: Electrical conductivity. F: Optical properties.

The nanometric particles selected according to Table 1 are submitted to a treatment for incorporating them in the final coating, for which it is possible to start from nanoparticles in aqueous, organic suspension or in powder form, without the compatibility between the vehicle of the nanoparticle and the base of the additive that is to be formulated being limiting, since an important part of the present invention is changing the vehicle in the additive to make it compatible with the final coating.

Referring to FIG. 1, which is a block diagram of the process for production of the additive of the invention, there are two zones, referenced with the numerals I and II: the first, made up of blocks (10) to (40), which represent a pretreatment of the nanoparticles, and the zone made up of blocks (50) and (60), representing the process of preparation of the additive as such.

In zone I or the pretreatment phase, block (10) represents the raw material, constituted of metal nanoparticles, their composites or mixtures thereof, which will be used for preparing the additive, preferably being a moist paste, although for some very specific applications that require absence of water, dry powder is preferred. As already mentioned, the nanoparticles have an average size in the range from 1 to 100 nanometers and a purity of at least 95%. This material is supplied to block (20).

Block (20) represents an operation designated “change of vehicle”, in which the raw material is washed for the purpose of removing the water or solvent contained, depending on the case, and replacing it with a “compatible” solvent, i.e. it is incorporated without causing phase separation, with the solvent or thinner of the final application (the “target coating”), which in its turn will prevent the formation of lumps on coming into contact with the target coating; the process is carried out with vigorous stirring preferably for between 5 and 30 minutes, or for as long as is necessary. The mixture is stirred in turbulent conditions by means of a disperser with a shearing disk or other device that provides a peripheral speed of at least 2 m/s and up to 30 m/s as a maximum. After stirring, phase separation takes place and the process can be repeated until a residual moisture content of less than 5% is obtained in the solid phase.

When because of the nature of the solvent or thinner, and of the resin contained in the target coating, the nanoparticles might react, the need for the particles to undergo a surface treatment (16) prior to the operation of “change of vehicle” (20), using conventional surfactants compatible with the target coating, is evaluated as indicated by block (15).

The process of “change of vehicle” (20) has the purpose of ensuring that the nanoparticles will not agglomerate in the dispersion phase (50) of zone II, on being incorporated in the coating or on application of the latter on the surface to be treated.

Block (30) indicates that in the case when the residual moisture content tolerated in the additive is very low, close to zero, owing to the nature of the resin and solvents or thinners in the target coating and once the stage of “change of vehicle” (20) is completed, the residual moisture content in the solid phase is reduced by a drying process (40), taking care that the operating temperature in said drying is below the boiling point of the vehicle. The operation is continued until a residual moisture content tolerated by the target coating is obtained.

The result of operation (40) is a “dry” powder of nanoparticles, which can be stored for subsequent preparation of the additive. The product obtained by this method retains its properties during prolonged periods of storage.

If a moisture content of the order of 5% is tolerated in the final application, the drying stage represented by block (40) is omitted.

The product obtained, whether “dry” or moist, resulting from one of the two routes of the first phase of the process (25) or (45), is submitted to a process of dispersion (50), in zone II, which properly is identified with preparation of the additive ready for use in the target coating according to the present invention.

In this stage, the paste or the “dry” powder from block (20) or (40) is fed to a process of dispersion (50) in which a resin and a dispersant that are compatible with the target coating are added, according to Table 2:

TABLE 2 Recommended selection of the resin and the dispersant for preparation of the additive RESIN CATEGORY RECOMMENDED DISPERSANT OF TARGET IN THE RECOMMENDED COATING DISPERSION IN THE DISPERSION Polyurethane Polyester copolymer with acid groups, or aldehyde alkylammonium salt of a polycarboxylic acid, alkylammonium salt of an unsaturated fatty acid, salt of unsaturated polyamine amides and acid polyesters of low molecular weight, unsaturated polyamine amide and acid polyesters of low molecular weight UV curing Epoxy- copolymer with acid groups, acrylate alkylammonium salt of a polycarboxylic acid, alkylammonium salt of an unsaturated fatty acid, salt of unsaturated polyamine amides and acid polyesters of low molecular weight, salt of an unsaturated polyamine amide and acid polyesters of low molecular weight Styrene - Styrene - ammonium salt of an acrylic Acrylic Acrylic copolymer, alkylammonium salt and a polyfunctional polymer of anionic character, sodium salt of an acrylic copolymer Vinylic Vinylic ammonium salt of an acrylic copolymer, alkylammonium salt and a polyfunctional polymer of anionic character, sodium salt of an acrylic copolymer Alkydalyl Alkydalyl copolymer with acid groups, enamel resin alkylammonium salt of a polycarboxylic acid, alkylammonium salt of an unsaturated fatty acid, salt of unsaturated polyamine amides and acid polyesters of low molecular weight, salt of an unsaturated polyamine amide and acid polyesters of low molecular weight 0% Styrene - ammonium salt of an acrylic Volatile Acrylic, copolymer, alkylammonium salt organic Vinylic, and a polyfunctional polymer of compounds Epoxy- anionic character, sodium salt acrylate of an acrylic copolymer Nitro- Stabilized copolymer with acid groups, cellulosic alkydalyl alkylammonium salt of a or nitro- polycarboxylic acid, cellulose alkylammonium salt of an unsaturated fatty acid, salt of unsaturated polyamine amides and acid polyesters of low molecular weight, salt of an unsaturated polyamine amide and acid polyesters of low molecular weight Alkydalyl Alkydalyl copolymer with acid groups, of soya, alkylammonium salt of a coconut, polycarboxylic acid, lecithin alkylammonium salt of an unsaturated fatty acid, salt of unsaturated polyamine amides and acid polyesters of low molecular weight, salt of an unsaturated polyamine amide and acid polyesters of low molecular weight Phenolic Phenolic copolymer with acid groups, resin alkylammonium salt of a polycarboxylic acid, alkylammonium salt of an unsaturated fatty acid, salt of unsaturated polyamine amides and acid polyesters of low molecular weight, salt of an unsaturated polyamine amide and acid polyesters of low molecular weight

Dispersion (50) is carried out by means of a stirrer or disperser with a peripheral speed of between 15 and 30 m/s. The viscosity of the mixture is adjusted to that of the target coating by adding solvent or thinner, which preferably is the same as will be used with the coating or at least must be compatible with it. The percentage of dispersant in the mixture is maintained at between 0.5 and 10% depending on the nanoparticles in the dry base.

The product (60) obtained from the process of dispersion (50) is the additive of the invention, and can even be, in the preferred embodiment, a formulation with up to 99 wt. % of nanoparticles.

Among the advantages of the additive obtained by the method of the invention, there is the fact that as a result of the treatment of change of vehicle in stage (20) and mixing with resins and dispersants in stage (50), the product is completely compatible with the target coating for which it was prepared by selecting the appropriate resin and dispersant in accordance with Table 2 presented above, and selection of a suitable surfactant, when necessary, moreover maintaining a high degree of homogeneity in the dispersion of nanoparticles in the formulation, so that on being added to the target coating, the additive will be incorporated easily and quickly and this ensures that the particles will maintain their homogeneity of dispersion throughout the volume and, therefore, in the coating layer after application on the surface to be protected.

Example 1 Preparation of the Additive for Use in an Organic Matrix for Use in Polyester-Based Paint

-   -   1. Start with a paste of nanoparticles of metallic silver, with         a water content of 64%, with a particle size distribution D₁₀,         16.3 nm; D₅₀, 23.9 nm; D₉₀, 43.5 nm; measured by photon         correlation spectroscopy (PCS), in equipment of type MALVERN         Zetasizer Nano ZS. For purposes of illustration, 300 grams is         used.     -   2. Pour the paste of nanoparticles into a narrow-mouth beaker of         the Berzelius type, equipped with a propeller disperser, add two         volumes of cellosolve butyl solvent, equal to that of the paste.         Disperse for 5 minutes.     -   3. Separate the nanoparticles from the mother liquor, by         physical means (decanting, filtration, centrifugation, etc.).         Retain the liquor for analysis of physical water by the Karl         Fischer method. Weigh the amount of paste of nanoparticles         obtained, to calculate the water content of the paste.     -   4. Repeat steps 2 and 3 as many times as necessary until, in the         paste of nanoparticles, a water content of less than 5%, or that         accepted for the final application, is reached.     -   5. Steps 2 and 3 are repeated 3 more times, but now the solvent         is replaced with propylene glycol acetate methyl ether.     -   6. In a separate vessel, dissolve 125 grams of the         polyester-based resin or some other that is compatible with this         system, for example, Laropal® A 81 (BASF), with 100 mL of the         solvent propylene glycol acetate methyl ether. Check for         complete dissolution of the resin by conventional methods.     -   7. Disperse the paste of nanoparticles obtained in step 5, in         the solution of resin and solvent from step 6, add 20 g of         dispersant, from the selection recommended in Table 2. A         peripheral speed of between 15 and 30 m/s for a period of         between 5 and 30 minutes is recommended. Verify dispersion of         the paste by known conventional methods.     -   8. Dilute the rest of the resin (375 grams) in the paste         dispersed in step 7, add a further 400 mL of solvent propylene         glycol acetate methyl ether. This is carried out for 1 hour at a         peripheral speed of 5 m/s.     -   9. Adjust the paste to 1000 grams with solvent propylene glycol         acetate methyl ether. Verify, in the paste, the percentage of         nanoparticles, the percentage of total solids, density,         viscosity, morphology by microscopy and physical moisture by         Karl Fischer.

Example 2 Preparation of the Additive for Use in an Organic Matrix for Use in Polyurethane-Based Paint

-   -   1. Start with a paste of nanoparticles of metallic silver, with         a water content of 64%, with a particle size distribution D₁₀,         16.3 nm; D₅₀, 23.9 nm; D₉₀, 43.5 nm; measured by photon         correlation spectroscopy (PCS), in equipment of type MALVERN         Zetasizer Nano ZS. For purposes of illustration, 300 grams is         used.     -   2. Pour the paste of nanoparticles into a narrow-mouth beaker of         the Berzelius type, equipped with a propeller disperser, add two         volumes of cellosolve butyl solvent, equal to that of the paste.         Disperse for a period of 5 minutes.     -   3. Separate the nanoparticles from the mother liquor, by         physical means (decanting, filtration, centrifugation, etc.).         Retain the liquor for analysis of physical water by the Karl         Fischer method. Weigh the amount of paste of nanoparticles         obtained, to calculate the water content of the paste.     -   4. Repeat steps 2 and 3 as many times as is necessary until, in         the paste of nanoparticles, a water content of less than 5% or         that accepted for the final application is reached.     -   5. In a separate vessel dissolve 125 grams of the         polyurethane-based resin or some other that is compatible with         this system, for example, Laropal® A 81 (BASF), with 100 mL of         the cellosolve butyl solvent. Check for complete dissolution of         the resin by conventional methods.     -   6. Disperse the paste of nanoparticles obtained in step 5, in         the solution of resin and solvent from step 6, add 20 g of         dispersant, from the selection recommended in Table 2. A         peripheral speed of between 15 and 30 m/s for a period of         between 5 and 30 minutes is recommended. Verify the dispersion         of the paste by known conventional methods.     -   7. Dilute the rest of the resin (375 grams) in the paste         dispersed in step 7, add a further 400 mL of cellosolve butyl         solvent. This is carried out for 1 hour at a peripheral speed of         5 m/s.     -   8. Adjust the paste to 1000 grams with cellosolve butyl solvent.         Verify, in the paste, the percentage of nanoparticles, the         percentage of total solids, density, viscosity, morphology by         microscopy and physical moisture by Karl Fischer.

As will be evident to a person skilled in the art, the process described for the production of the additive according to the present invention can be used for obtaining suitable additives that confer desired properties in the final application, by selecting the compound or mixture of compounds according to Table 1, without the need to modify the method. It will also be evident that other elements or their compounds can be used for conferring these or other properties in the same method of manufacture. 

1-9. (canceled)
 10. A method of preparation of an additive for coatings intended for protecting surfaces, the active agent of the additive being a metal, its compounds or mixtures thereof, said method being characterized in that it comprises a first phase of pretreatment of the active agent and a second phase of preparation of the additive, where: i) in the first pretreatment phase, the water content of the active agent is reduced if necessary, replacing it with a vehicle that is compatible with the coating (“change of vehicle”), and ii) in the second phase, a dispersion of the pretreated active agent is prepared, mixing it with a resin, a dispersant and a solvent compatible with said coating.
 11. (canceled)
 12. The method of preparation of an additive as claimed in claim 10, characterized in that in the first pretreatment phase, the moisture contained in the active agent is replaced with a vehicle compatible with the diluent of the coating, by washing the initial active agent with the compatible vehicle.
 13. The method of preparation of an additive as claimed in claim 12, characterized in that the washing is carried out with vigorous stirring preferably with a peripheral speed between 5 m/s and 30 m/s and for a length of time between 5 and 30 minutes.
 14. The method of preparation of an additive as claimed in claim 13, further characterized in that the washing is repeated until the water content required for the application is obtained.
 15. The method of preparation of an additive as claimed in claim 12, further characterized in that if the active agent is likely to react with the coating, the active agent is submitted to a surface treatment with surfactants, prior to washing.
 16. The method of preparation of an additive as claimed in claim 10, characterized in that when the residual moisture content permitted for the coating is close to zero, the product obtained from the “change of vehicle” in the pretreatment phase is submitted to a drying process.
 17. The method of preparation of an additive as claimed in claim 10, characterized in that the metallic compound obtained from the first pretreatment phase has a water content between 0% and 5%, and is dispersible in a resin compatible with the target coating.
 18. The method of preparation of an additive as claimed in claim 10, characterized in that dispersion is carried out at a peripheral speed of between 15 and 30 m/s.
 19. The method of preparation of an additive as claimed in claim 10, characterized in that the percentage of dispersant in the mixture is maintained at between 0.5 and 10% based on the active agent.
 20. The method of preparation of an additive as claimed in claim 10, characterized in that the product obtained is an additive that contains up to 99 wt. % of nanometric compound as active agent.
 21. The method of preparation of an additive as claimed in claim 13, characterized in that after stirring the phases are separated, the liquid phase being removed. 